Canonical Allele Identifier: PA2825640021
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730350
ClinVar RCV Id: RCV002326526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1094Lys
CA16028645
NM_001127511.3:c.3281C>A